intriguing association with rs10251794 (P = 3.43 × 10−5), an intronic SNP in CNTNAP2, which encodes for the member of the neurexin family that has been linked with autism (68-70) and a complex phenotype of schizophrenia, epilepsy, and cognitive impairment (71). Other genes with strong signals and plausible biological relevance are the brain-specific angiogenesis inhibitor 3 (BAI3; rs9342730; P = 1.22 × 10−5) and the myelin oligodendrocyte glycoprotein (MOG; rs16895223; P = 4.60 × 10−5).
